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Langerhans cell histiocytosis [PDF]
The authors present a rare case of Langerhans cell histiocytosis in a 31 year old female patient with vulvar, peri-anal and oral lesions, diabetes insipidus, pulmonary skin and bone infiltrations.
Maria de Lourdes L. F. Chauffaille+10 more
doaj +11 more sources
Langerhans‐Cell Histiocytosis [PDF]
Langerhans cell histiocytosis (LCH) formerly known as pulmonary eosinophilic granuloma is currently regarded by the World Health Organization as a clonal neoplastic proliferation of histiocytes.
C. Allen, M. Merad, K. McClain
semanticscholar +6 more sources
Langerhans Cell histiocytosis. [PDF]
Langerhans Cell Histiocytosis (LCH) is caused by clonal expansion of myeloid precursors that differentiate into CD1a+/CD207+ cells in lesions that leads to a spectrum of organ involvement and dysfunction.
C. Rodríguez-Galindo, C. Allen
semanticscholar +4 more sources
Background Langerhans cells belong to the histiocytic system and give rise to two tumors: Langerhans cell histiocytosis and Langerhans cell sarcoma. Clinical aggressiveness and degree of atypia distinguish the two neoplasms. Langerhans cell histiocytosis
Marah Hamdan, Jesse C. Qiao, Vid Fikfak
doaj +2 more sources
Langerhans Cell Histiocytosis [PDF]
Adult onset Langerhans cell histiocytosis is uncommon. A 29 year old man is presented who developed classic cutaneous disease with severe systemic involvement. He responded completely to a two month course of thalidomide.
Geraldine S. Pinkus+5 more
openalex +5 more sources
Polyostotic Langerhans cell histiocytosis presenting as halitosis in a 24-year-old man: a case report [PDF]
Background Langerhans cell histiocytosis is a rare disease of the reticuloendothelial system. This report presents a novel case of Langerhans cell histiocytosis with systemic involvement that started with a simple chief complaint.
Hassan Mirmohammad Sadeghi+6 more
doaj +2 more sources
Insights into etiology and management of a case of Langerhans cell histiocytosis manifesting as perianal lesions: a case report [PDF]
Background Langerhans cell histiocytosis is a rare disorder characterized by abnormal proliferation of Langerhans cells, primarily affecting children and occasionally adults.
Pei Xiao-yue, Tai Zixin, Zhang Wen-jun
doaj +2 more sources
Langerhans' cell histiocytosis in adults [PDF]
Three cases of Langerhans' cell histiocytosis with unusual clinical and histopathologic features are described. The first two cases illustrate diagnostic pitfalls that underscore the importance of considering Langerhans' cell histiocytosis in the differential diagnosis of purpuric papular eruptions of the scalp and intertriginous areas, particularly in
Fiorina Giona+9 more
openalex +4 more sources
Langerhans cell histiocytosis is a rare proliferative disease of histiocyte-like cells, the peak incidence of which occurs in early childhood. Pulmonary Langerhans Cell Histiocytosis is one of the forms of this disease, but it usually affects young ...
Victor V. Fomin+4 more
doaj +2 more sources
Langerhans cell histiocytosis [PDF]
Richard D. Brunning
openalex +4 more sources